ID: ALA3235634

Max Phase: Preclinical

Molecular Formula: C32H29Cl2N5O2

Molecular Weight: 586.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(Oc2ccccc2N/C(=N/c2ccc(Cl)cc2)NCCCNc2ccnc3cc(Cl)ccc23)cc1

Standard InChI:  InChI=1S/C32H29Cl2N5O2/c1-40-25-12-14-26(15-13-25)41-31-6-3-2-5-29(31)39-32(38-24-10-7-22(33)8-11-24)37-19-4-18-35-28-17-20-36-30-21-23(34)9-16-27(28)30/h2-3,5-17,20-21H,4,18-19H2,1H3,(H,35,36)(H2,37,38,39)

Standard InChI Key:  QWOFTNRIHMKLIO-UHFFFAOYSA-N

Associated Targets(non-human)

Sporothrix schenckii 1580 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Klebsiella pneumoniae 43867 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cryptococcus neoformans 21258 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Plasmodium falciparum 966862 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Trichophyton mentagrophytes 4846 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus fumigatus 16427 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida parapsilosis 8521 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 586.52Molecular Weight (Monoisotopic): 585.1698AlogP: 8.53#Rotatable Bonds: 10
Polar Surface Area: 79.80Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 7.78CX LogP: 7.08CX LogD: 6.45
Aromatic Rings: 5Heavy Atoms: 41QED Weighted: 0.09Np Likeness Score: -1.16

References

1. Mishra A, Batchu H, Srivastava K, Singh P, Shukla PK, Batra S..  (2014)  Synthesis and evaluation of new diaryl ether and quinoline hybrids as potential antiplasmodial and antimicrobial agents.,  24  (7): [PMID:24630564] [10.1016/j.bmcl.2014.02.044]

Source